Congenital disorders of glycosylation. Part I. Defects of protein N-glycosylation.
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Synaptic roles for phosphomannomutase type 2 in a new Drosophila congenital disorder of glycosylation disease modelUnconventional secretory processing diversifies neuronal ion channel properties.A mouse model of a human congenital disorder of glycosylation caused by loss of PMM2.Differential site accessibility mechanistically explains subcellular-specific N-glycosylation determinants.N-glycosylation of R-spondin1 at Asn137 negatively regulates its secretion and Wnt/β-catenin signaling-enhancing activity.Diseases associated with N-glycosylation of proteins
P2860
Congenital disorders of glycosylation. Part I. Defects of protein N-glycosylation.
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article científic
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article scientifique
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articol științific
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articolo scientifico
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artigo científico
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artigo científico
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artigo científico
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Congenital disorders of glycosylation. Part I. Defects of protein N-glycosylation.
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label
Congenital disorders of glycosylation. Part I. Defects of protein N-glycosylation.
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prefLabel
Congenital disorders of glycosylation. Part I. Defects of protein N-glycosylation.
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P2093
P1476
Congenital disorders of glycosylation. Part I. Defects of protein N-glycosylation.
@en
P2093
Bogdan Cylwik
Ewa Gruszewska
Lech Chrostek
Marcin Naklicki
P304
P577
2013-05-31T00:00:00Z